Ortholog genes from cactophilic Drosophila provide insight into human adaptation to hallucinogenic cacti.
PMID:35915153
Strongly Truncated Dnaaf4 Plays a Conserved Role in Drosophila Ciliary Dynein Assembly as Part of an R2TP-Like Co-Chaperone Complex With Dnaaf6.
PMID:35873488
A Drosophila melanogaster model for TMEM43-related arrhythmogenic right ventricular cardiomyopathy type 5.
PMID:35869176
The E3 ligase Thin controls homeostatic plasticity through neurotransmitter release repression.
PMID:35796533
The evolution of vitamin C biosynthesis and transport in animals.
PMID:35752765
Functional Studies of Genetic Variants Associated with Human Diseases in Notch Signaling-Related Genes Using Drosophila.
PMID:35674905
Assessing the Roles of Potential Notch Signaling Components in Instructive and Permissive Pathways with Two Drosophila Pericardial Reporters.
PMID:35674896
GRNbenchmark - a web server for benchmarking directed gene regulatory network inference methods.
PMID:35609981
The Quest for Orthologs orthology benchmark service in 2022.
PMID:35552456
Concurrent outcomes from multiple approaches of epistasis analysis for human body mass index associated loci provide insights into obesity biology.
PMID:35508500
The myokine Fibcd1 is an endogenous determinant of myofiber size and mitigates cancer-induced myofiber atrophy.
PMID:35501350
Trans-omics analysis of insulin action reveals a cell growth subnetwork which co-regulates anabolic processes.
PMID:35494245
Coexpression reveals conserved gene programs that co-vary with cell type across kingdoms.
PMID:35451481
A translation control module coordinates germline stem cell differentiation with ribosome biogenesis during Drosophila oogenesis.
PMID:35413237
Disease Modeling of Rare Neurological Disorders in Zebrafish.
PMID:35409306
Predicted mouse interactome and network-based interpretation of differentially expressed genes.
PMID:35390003
Harmonizing model organism data in the Alliance of Genome Resources.
PMID:35380658
JaponicusDB: rapid deployment of a model organism database for an emerging model species.
PMID:35380656
Maintenance of mitochondrial integrity in midbrain dopaminergic neurons governed by a conserved developmental transcription factor.
PMID:35301315
Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases.
PMID:35294868
Inter-Species Rescue of Mutant Phenotype-The Standard for Genetic Analysis of Human Genetic Disorders in Drosophila melanogaster Model.
PMID:35269756
FlyBase: a guided tour of highlighted features.
PMID:35266522
Using Drosophila Nephrocytes to Understand the Formation and Maintenance of the Podocyte Slit Diaphragm.
PMID:35265622
Invertebrate Model Organisms as a Platform to Investigate Rare Human Neurological Diseases.
PMID:35256540
Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures.
PMID:35240055
Genetics and Brain Transcriptomics of Completed Suicide.
PMID:35236118
ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research.
PMID:35224820
Glia fuel neurons with locally synthesized ketone bodies to sustain memory under starvation.
PMID:35177854
Dynamics of huntingtin protein interactions in the striatum identifies candidate modifiers of Huntington disease.
PMID:35148841
WormBase in 2022-data, processes, and tools for analyzing Caenorhabditis elegans.
PMID:35134929
Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling.
PMID:35044823
SLC22 Transporters in the Fly Renal System Regulate Response to Oxidative Stress In Vivo.
PMID:34948211
Temporal Profiling of the Cortical Synaptic Mitochondrial Proteome Identifies Ageing Associated Regulators of Stability.
PMID:34943911
A cis-regulatory-directed pipeline for the identification of genes involved in cardiac development and disease.
PMID:34906219
New data and collaborations at the Saccharomyces Genome Database: updated reference genome, alleles, and the Alliance of Genome Resources.
PMID:34897464
Drosophila Trachea as a Novel Model of COPD.
PMID:34884534
Modulation of retinoid-X-receptors differentially regulates expression of apolipoprotein genes apoc1 and apoeb by zebrafish microglia.
PMID:34878094
Cross-species analysis of viral nucleic acid interacting proteins identifies TAOKs as innate immune regulators.
PMID:34853303
A Drosophila RNAi screen reveals conserved glioblastoma-related adhesion genes that regulate collective cell migration.
PMID:34849760
Bioinformatic and cell-based tools for pooled CRISPR knockout screening in mosquitos.
PMID:34819517
Echinobase: leveraging an extant model organism database to build a knowledgebase supporting research on the genomics and biology of echinoderms.
PMID:34791383
A large-scale transgenic RNAi screen identifies transcription factors that modulate myofiber size in Drosophila.
PMID:34780463
Metabolic resistance to the inhibition of mitochondrial transcription revealed by CRISPR-Cas9 screen.
PMID:34779571
Predicting novel candidate human obesity genes and their site of action by systematic functional screening in Drosophila.
PMID:34748544
An integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients.
PMID:34746695
Loxl2 is a mediator of cardiac aging in Drosophila melanogaster, genetically examining the role of aging clock genes.
PMID:34734976
Spatially resolved transcriptomics reveals the architecture of the tumor-microenvironment interface.
PMID:34725363
ConVarT: a search engine for matching human genetic variants with variants from non-human species.
PMID:34718716
Mouse Genome Informatics (MGI): latest news from MGD and GXD.
PMID:34698891
The conserved fertility factor SPACA4/Bouncer has divergent modes of action in vertebrate fertilization.
PMID:34556579
Circadian regulation of the Drosophila astrocyte transcriptome.
PMID:34543266
Cooperation between melanoma cell states promotes metastasis through heterotypic cluster formation.
PMID:34529939
A scalable Drosophila assay for clinical interpretation of human PTEN variants in suppression of PI3K/AKT induced cellular proliferation.
PMID:34492006
Phosphatidylserine synthase plays an essential role in glia and affects development, as well as the maintenance of neuronal function.
PMID:34401677
Tumour-host interactions through the lens of Drosophila.
PMID:34389815
A nomenclature for echinoderm genes.
PMID:34386815
Identification of conserved transcriptome features between humans and Drosophila in the aging brain utilizing machine learning on combined data from the NIH Sequence Read Archive.
PMID:34379632
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.
PMID:34314705
Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster.
PMID:34274978
Transcriptome analysis of chloride intracellular channel knockdown in Drosophila identifies oxidation-reduction function as possible mechanism of altered sensitivity to ethanol sedation.
PMID:34228751
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11.
PMID:34113007
RAL GTPases mediate EGFR-driven intestinal stem cell proliferation and tumourigenesis.
PMID:34096503
The foraging gene affects alcohol sensitivity, metabolism and memory in Drosophila.
PMID:34092172
Genetic basis of variation in cocaine and methamphetamine consumption in outbred populations of Drosophila melanogaster.
PMID:34074789
Alcohol-induced aggression in Drosophila.
PMID:34044470
The epigenetic regulator G9a attenuates stress-induced resistance and metabolic transcriptional programs across different stressors and species.
PMID:34030685
Integration of 1:1 orthology maps and updated datasets into Echinobase.
PMID:34010390
DRscDB: A single-cell RNA-seq resource for data mining and data comparison across species.
PMID:33995899
Functional conservation in genes and pathways linking ageing and immunity.
PMID:33990202
Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision.
PMID:33962631
Updates to HCOP: the HGNC comparison of orthology predictions tool.
PMID:33959747
Proteomics of protein trafficking by in vivo tissue-specific labeling.
PMID:33888706
Downregulation of glial genes involved in synaptic function mitigates Huntington's disease pathogenesis.
PMID:33871358
Receptors and Channels Associated with Alcohol Use: Contributions from Drosophila.
PMID:33870197
Rare deleterious de novo missense variants in Rnf2/Ring2 are associated with a neurodevelopmental disorder with unique clinical features.
PMID:33864376
Functional assessment of the "two-hit" model for neurodevelopmental defects in Drosophila and X. laevis.
PMID:33819264
Cellular Control of Protein Turnover via the Modification of the Amino Terminus.
PMID:33805528
Natural genetic variation in Drosophila melanogaster reveals genes associated with Coxiella burnetii infection.
PMID:33789347
TDP-43 and PINK1 mediate CHCHD10S59L mutation-induced defects in Drosophila and in vitro.
PMID:33772006
Functional analysis of SARS-CoV-2 proteins in Drosophila identifies Orf6-induced pathogenic effects with Selinexor as an effective treatment.
PMID:33766136
TDP-43 proteinopathy alters the ribosome association of multiple mRNAs including the glypican Dally-like protein (Dlp)/GPC6.
PMID:33762006
Natural variation in the regulation of neurodevelopmental genes modifies flight performance in Drosophila.
PMID:33735180
HIR V2: a human interactome resource for the biological interpretation of differentially expressed genes via gene set linkage analysis.
PMID:33677507
Mayday sustains trans-synaptic BMP signaling required for synaptic maintenance with age.
PMID:33667157
Stable Isotope Labeling of Amino Acids in Flies (SILAF) Reveals Differential Phosphorylation of Mitochondrial Proteins Upon Loss of OXPHOS Subunits.
PMID:33640490
Exocyst-mediated membrane trafficking of the lissencephaly-associated ECM receptor dystroglycan is required for proper brain compartmentalization.
PMID:33620318
Shape deformation analysis reveals the temporal dynamics of cell-type-specific homeostatic and pathogenic responses to mutant huntingtin.
PMID:33618800
The one-carbon pool controls mitochondrial energy metabolism via complex I and iron-sulfur clusters.
PMID:33608280
The chromatin remodeler ISWI acts during Drosophila development to regulate adult sleep.
PMID:33597246
Cross-species identification of PIP5K1-, splicing- and ubiquitin-related pathways as potential targets for RB1-deficient cells.
PMID:33591981
Harnessing the paradoxical phenotypes of APOE ɛ2 and APOE ɛ4 to identify genetic modifiers in Alzheimer's disease.
PMID:33576571
The extracellular matrix phenome across species.
PMID:33543035
In-silico definition of the Drosophila melanogaster matrisome.
PMID:33543012
SATB2 induction of a neural crest mesenchyme-like program drives melanoma invasion and drug resistance.
PMID:33527896
Prediction of complex phenotypes using the Drosophila melanogaster metabolome.
PMID:33510469
Slowed Protein Turnover in Aging Drosophila Reflects a Shift in Cellular Priorities.
PMID:33453098
Downregulation of the tyrosine degradation pathway extends Drosophila lifespan.
PMID:33319750
Biotin rescues mitochondrial dysfunction and neurotoxicity in a tauopathy model.
PMID:33318181
Comparative proteomic analysis highlights metabolic dysfunction in α-synucleinopathy.
PMID:33311497
Identification of Genes Contributing to a Long Circadian Period in Drosophila Melanogaster.
PMID:33274675
In silico identification of Drosophila melanogaster genes encoding RNA polymerase subunits.
PMID:33274328
An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder.
PMID:33261099
BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms.
PMID:33232675
FlyBase: updates to the Drosophila melanogaster knowledge base.
PMID:33219682
Predicted rat interactome database and gene set linkage analysis.
PMID:33216897
Dynamic changes in the brain protein interaction network correlates with progression of Aβ42 pathology in Drosophila.
PMID:33116184
FlyRNAi.org-the database of the Drosophila RNAi screening center and transgenic RNAi project: 2021 update.
PMID:33104800
Predicted functional interactome of Caenorhabditis elegans and a web tool for the functional interpretation of differentially expressed genes.
PMID:33076954
The Drosophila seminal proteome and its role in postcopulatory sexual selection.
PMID:33070726
Alcohol Sensitivity as an Endophenotype of Alcohol Use Disorder: Exploring Its Translational Utility between Rodents and Humans.
PMID:33066036
Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart.
PMID:33033063
BioLitMine: Advanced Mining of Biomedical and Biological Literature About Human Genes and Genes from Major Model Organisms.
PMID:33028629
Patient-specific genomics and cross-species functional analysis implicate LRP2 in hypoplastic left heart syndrome.
PMID:33006316
Integrated analysis of the aging brain transcriptome and proteome in tauopathy.
PMID:32993812
Dynamics of a Protein Interaction Network Associated to the Aggregation of polyQ-Expanded Ataxin-1.
PMID:32992839
SWI/SNF complexes act through CBP-1 histone acetyltransferase to regulate acute functional tolerance to alcohol.
PMID:32957927
Analysis of brain region-specific co-expression networks reveals clustering of established and novel genes associated with Alzheimer disease.
PMID:32878640
Drosophila and its gut microbes: a model for drug-microbiome interactions.
PMID:32855644
Predictive features of gene expression variation reveal mechanistic link with differential expression.
PMID:32767663
miR-92a Suppresses Mushroom Body-Dependent Memory Consolidation in Drosophila.
PMID:32737186
Genetic and metabolomic architecture of variation in diet restriction-mediated lifespan extension in Drosophila.
PMID:32644988
A Genetic Analysis of Tumor Progression in Drosophila Identifies the Cohesin Complex as a Suppressor of Individual and Collective Cell Invasion.
PMID:32629605
Drosophila models of pathogenic copy-number variant genes show global and non-neuronal defects during development.
PMID:32579612
Piwi reduction in the aged niche eliminates germline stem cells via Toll-GSK3 signaling.
PMID:32561720
Automated generation of gene summaries at the Alliance of Genome Resources.
PMID:32559296
An Unbiased Drug Screen for Seizure Suppressors in Duplication 15q Syndrome Reveals 5-HT1A and Dopamine Pathway Activation as Potential Therapies.
PMID:32507391
Frameshift mutations of YPEL3 alter the sensory circuit function in Drosophila.
PMID:32461240
Intron and gene size expansion during nervous system evolution.
PMID:32410625
The Quest for Orthologs benchmark service and consensus calls in 2020.
PMID:32374845
Protein phosphatase 1 activity controls a balance between collective and single cell modes of migration.
PMID:32369438
De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment.
PMID:32356556
CRISPR/Cas9 mediated genetic resource for unknown kinase and phosphatase genes in Drosophila.
PMID:32355295
Drosophila as a model for studying cystic fibrosis pathophysiology of the gastrointestinal system.
PMID:32345720
Amyotrophic Lateral Sclerosis Modifiers in Drosophila Reveal the Phospholipase D Pathway as a Potential Therapeutic Target.
PMID:32345615
Analysis of genes within the schizophrenia-linked 22q11.2 deletion identifies interaction of night owl/LZTR1 and NF1 in GABAergic sleep control.
PMID:32339168
Variants in CAPZA2, a member of an F-actin capping complex, cause intellectual disability and developmental delay.
PMID:32338762
De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy.
PMID:32330417
Cdk1 Controls Global Epigenetic Landscape in Embryonic Stem Cells.
PMID:32240602
A widespread family of heat-resistant obscure (Hero) proteins protect against protein instability and aggregation.
PMID:32163402
Alcohol Causes Lasting Differential Transcription in Drosophila Mushroom Body Neurons.
PMID:32132098
A Connected Network of Interacting Proteins Is Involved in Human-Tau Toxicity in Drosophila.
PMID:32116515
The conserved microRNA miR-34 regulates synaptogenesis via coordination of distinct mechanisms in presynaptic and postsynaptic cells.
PMID:32107390
Predicted Drosophila Interactome Resource and web tool for functional interpretation of differentially expressed genes.
PMID:32103267
Identifying conserved molecular targets required for cell migration of glioblastoma cancer stem cells.
PMID:32102991
Large-Scale Transgenic Drosophila Resource Collections for Loss- and Gain-of-Function Studies.
PMID:32071193
Reduced Function of the Glutathione S-Transferase S1 Suppresses Behavioral Hyperexcitability in Drosophila Expressing Mutant Voltage-Gated Sodium Channels.
PMID:32054635
NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models.
PMID:32053595
Chondroitin sulfate proteoglycan Windpipe modulates Hedgehog signaling in Drosophila.
PMID:32049582
Genetic interaction screen for severe neurodevelopmental disorders reveals a functional link between Ube3a and Mef2 in Drosophila melanogaster.
PMID:31988313
Profiling of the muscle-specific dystroglycan interactome reveals the role of Hippo signaling in muscular dystrophy and age-dependent muscle atrophy.
PMID:31959160
The DNA polymerases of Drosophila melanogaster.
PMID:31933406
A cell atlas of the adult Drosophila midgut.
PMID:31915294
Straightjacket/α2δ3 deregulation is associated with cardiac conduction defects in myotonic dystrophy type 1.
PMID:31829940
Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction.
PMID:31785787
Glycogen branching enzyme controls cellular iron homeostasis via Iron Regulatory Protein 1 and mitoNEET.
PMID:31784520
Functional conservation of RecQ helicase BLM between humans and Drosophila melanogaster.
PMID:31772289
A Genetic Screen for Genes That Impact Peroxisomes in Drosophila Identifies Candidate Genes for Human Disease.
PMID:31767637
Genetic architecture of subcortical brain structures in 38,851 individuals.
PMID:31636452
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders.
PMID:31616000
Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature.
PMID:31607425
Next-Generation Genome-Scale Models Incorporating Multilevel 'Omics Data: From Yeast to Human.
PMID:31602621
HELZ directly interacts with CCR4-NOT and causes decay of bound mRNAs.
PMID:31570513
Forward genetic screen in human podocytes identifies diphthamide biosynthesis genes as regulators of adhesion.
PMID:31566424
Alliance of Genome Resources Portal: unified model organism research platform.
PMID:31552413
Using MARRVEL v1.2 for Bioinformatics Analysis of Human Genes and Variant Pathogenicity.
PMID:31524990
Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information.
PMID:31475990
An RNAi Screen for Genes Required for Growth of Drosophila Wing Tissue.
PMID:31387856
A Key Role for the Ubiquitin Ligase UBR4 in Myofiber Hypertrophy in Drosophila and Mice.
PMID:31365869
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia.
PMID:31327508
A Cyclin A-Myb-MuvB-Aurora B network regulates the choice between mitotic cycles and polyploid endoreplication cycles.
PMID:31291240
Glial α-synuclein promotes neurodegeneration characterized by a distinct transcriptional program in vivo.
PMID:31267577
Convergent Evidence From Humans and Drosophila melanogaster Implicates the Transcription Factor MEF2B/Mef2 in Alcohol Sensitivity.
PMID:31241765
Advances and Applications in the Quest for Orthologs.
PMID:31241141
The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance.
PMID:31230720
The fruit fly at the interface of diagnosis and pathogenic mechanisms of rare and common human diseases.
PMID:31227826
Endocrine regulation of MFS2 by branchless controls phosphate excretion and stone formation in Drosophila renal tubules.
PMID:31217461
Characterizing building blocks of resource constrained biological networks.
PMID:31216986
CAPRI enables comparison of evolutionarily conserved RNA interacting regions.
PMID:31213602
STRIPAK Members Orchestrate Hippo and Insulin Receptor Signaling to Promote Neural Stem Cell Reactivation.
PMID:31167138
Direct role for the Drosophila GIGYF protein in 4EHP-mediated mRNA repression.
PMID:31114929
A Comprehensive Drosophila melanogaster Transcription Factor Interactome.
PMID:30995488
Rare variants in MYH15 modify amyotrophic lateral sclerosis risk.
PMID:30985904
Expressional Profiling of Carpet Glia in the Developing Drosophila Eye Reveals Its Molecular Signature of Morphology Regulators.
PMID:30983950
Enabling cell-type-specific behavioral epigenetics in Drosophila: a modified high-yield INTACT method reveals the impact of social environment on the epigenetic landscape in dopaminergic neurons.
PMID:30967153
Sterol regulatory element binding protein 1 couples mechanical cues and lipid metabolism.
PMID:30902980
Glass confers rhabdomeric photoreceptor identity in Drosophila, but not across all metazoans.
PMID:30873275
Increased intron retention is a post-transcriptional signature associated with progressive aging and Alzheimer's disease.
PMID:30868713
Autophagy accounts for approximately one-third of mitochondrial protein turnover and is protein selective.
PMID:30865561
Survey of the Ciliary Motility Machinery of Drosophila Sperm and Ciliated Mechanosensory Neurons Reveals Unexpected Cell-Type Specific Variations: A Model for Motile Ciliopathies.
PMID:30774648
Ion Channel Contributions to Wing Development in Drosophila melanogaster.
PMID:30733380
Towards comprehensive annotation of Drosophila melanogaster enzymes in FlyBase.
PMID:30689844
RiboTag translatomic profiling of Drosophila oenocytes under aging and induced oxidative stress.
PMID:30651069
Assigning confidence scores to homoeologs using fuzzy logic.
PMID:30648004
Meta-analysis of Genetic Modifiers Reveals Candidate Dysregulated Pathways in Amyotrophic Lateral Sclerosis.
PMID:30594291
Putative contributions of the sex chromosome proteins SOX3 and SRY to neurodevelopmental disorders.
PMID:30537354
Variants in PUS7 Cause Intellectual Disability with Speech Delay, Microcephaly, Short Stature, and Aggressive Behavior.
PMID:30526862
As time flies by: Investigating cardiac aging in the short-lived Drosophila model.
PMID:30496794
Quantifying Tissue-Specific Overexpression of FOXO in Drosophila via mRNA Fluorescence In Situ Hybridization Using Branched DNA Probe Technology.
PMID:30414154
Drosophila intestinal stem and progenitor cells are major sources and regulators of homeostatic niche signals.
PMID:30404917
iProteinDB: An Integrative Database of Drosophila Post-translational Modifications.
PMID:30397019
FlyBase 2.0: the next generation.
PMID:30364959
Genome-Wide Association Study of Circadian Behavior in Drosophila melanogaster.
PMID:30341464
The Proton-Coupled Monocarboxylate Transporter Hermes Is Necessary for Autophagy during Cell Death.
PMID:30318245
Glucocerebrosidase deficiency promotes protein aggregation through dysregulation of extracellular vesicles.
PMID:30256786
The CCHamide1 Neuropeptide Expressed in the Anterior Dorsal Neuron 1 Conveys a Circadian Signal to the Ventral Lateral Neurons in Drosophila melanogaster.
PMID:30246807
Model organism data evolving in support of translational medicine.
PMID:30224793
Dme-Hsa Disease Database (DHDD): Conserved Human Disease-Related miRNA and Their Targeting Genes in Drosophila melanogaster.
PMID:30200613
Using High-Throughput Animal or Cell-Based Models to Functionally Characterize GWAS Signals.
PMID:30147999
OrthoList 2: A New Comparative Genomic Analysis of Human and Caenorhabditis elegans Genes.
PMID:30120140
Conservation of kinase-phosphorylation site pairings: Evidence for an evolutionarily dynamic phosphoproteome.
PMID:30106995
Genes Involved in Drosophila melanogaster Ovarian Function Are Highly Conserved Throughout Evolution.
PMID:30060195
IRF2BPL Is Associated with Neurological Phenotypes.
PMID:30057031
Pooled genome-wide CRISPR screening for basal and context-specific fitness gene essentiality in Drosophila cells.
PMID:30051818
Microfluidics for mechanobiology of model organisms.
PMID:30037463
ProMotE: an efficient algorithm for counting independent motifs in uncertain network topologies.
PMID:29940838
Analysis of Drosophila STING Reveals an Evolutionarily Conserved Antimicrobial Function.
PMID:29924997
A Cyclin E Centered Genetic Network Contributes to Alcohol-Induced Variation in Drosophila Development.
PMID:29871898
Using Drosophila to study mechanisms of hereditary hearing loss.
PMID:29853544
Cell division cycle 7 kinase is a negative regulator of cell-mediated collagen degradation.
PMID:29792348
Using FlyBase to Find Functionally Related Drosophila Genes.
PMID:29761468
A high throughput, functional screen of human Body Mass Index GWAS loci using tissue-specific RNAi Drosophila melanogaster crosses.
PMID:29608557
Integrated biology approach reveals molecular and pathological interactions among Alzheimer's Aβ42, Tau, TREM2, and TYROBP in Drosophila models.
PMID:29598827
A gene-specific T2A-GAL4 library for Drosophila.
PMID:29565247
Using genetic buffering relationships identified in fission yeast to reveal susceptibilities in cells lacking hamartin or tuberin function.
PMID:29343513
The von Hippel-Lindau Gene Is Required to Maintain Renal Proximal Tubule and Glomerulus Integrity in Zebrafish Larvae.
PMID:29342457
The ABC Transporter Eato Promotes Cell Clearance in the Drosophila melanogaster Ovary.
PMID:29295819
The ModERN Resource: Genome-Wide Binding Profiles for Hundreds of Drosophila and Caenorhabditis elegans Transcription Factors.
PMID:29284660
Genotype Influences Day-to-Day Variability in Sleep in Drosophila melanogaster.
PMID:29228366
Zinc Detoxification: A Functional Genomics and Transcriptomics Analysis in Drosophila melanogaster Cultured Cells.
PMID:29223976
Improved detection of synthetic lethal interactions in Drosophila cells using variable dose analysis (VDA).
PMID:29183982
Molecular Interaction Search Tool (MIST): an integrated resource for mining gene and protein interaction data.
PMID:29155944
Proteomic profiling of neuronal mitochondria reveals modulators of synaptic architecture.
PMID:29078798
The Glia-Neuron Lactate Shuttle and Elevated ROS Promote Lipid Synthesis in Neurons and Lipid Droplet Accumulation in Glia via APOE/D.
PMID:28965825
Proteomic mapping of differentially vulnerable pre-synaptic populations identifies regulators of neuronal stability in vivo.
PMID:28963550
Identification of genetic networks that act in the somatic cells of the testis to mediate the developmental program of spermatogenesis.
PMID:28957323
A novel Drosophila injury model reveals severed axons are cleared through a Draper/MMP-1 signaling cascade.
PMID:28825401
Genome-wide identification of Grainy head targets in Drosophila reveals regulatory interactions with the POU domain transcription factor Vvl.
PMID:28760809
Regulation of Mitochondrial Complex I Biogenesis in Drosophila Flight Muscles.
PMID:28683319
Gene2Function: An Integrated Online Resource for Gene Function Discovery.
PMID:28663344
Genetics of alcohol consumption in Drosophila melanogaster.
PMID:28627812
Autophagy suppresses Ras-driven epithelial tumourigenesis by limiting the accumulation of reactive oxygen species.
PMID:28581519
Major hnRNP proteins act as general TDP-43 functional modifiers both in Drosophila and human neuronal cells.
PMID:28575377
Multifunctional glial support by Semper cells in the Drosophila retina.
PMID:28562601
Genomic Analysis of Genotype-by-Social Environment Interaction for Drosophila melanogaster Aggressive Behavior.
PMID:28550016
Ancient antagonism between CELF and RBFOX families tunes mRNA splicing outcomes.
PMID:28512194
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.
PMID:28502612
A Personalized Model of COQ2 Nephropathy Rescued by the Wild-Type COQ2 Allele or Dietary Coenzyme Q10 Supplementation.
PMID:28428331
Retrotransposon activation contributes to neurodegeneration in a Drosophila TDP-43 model of ALS.
PMID:28301478
Circadian deep sequencing reveals stress-response genes that adopt robust rhythmic expression during aging.
PMID:28221375
The Drosophila Gene Expression Tool (DGET) for expression analyses.
PMID:28187709
A Drosophila model system to assess the function of human monogenic podocyte mutations that cause nephrotic syndrome.
PMID:28164240
Drosophila and genome-wide association studies: a review and resource for the functional dissection of human complex traits.
PMID:28151408
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.
PMID:28137300
Genome-Scale Networks Link Neurodegenerative Disease Genes to α-Synuclein through Specific Molecular Pathways.
PMID:28131822
High throughput in vivo functional validation of candidate congenital heart disease genes in Drosophila.
PMID:28084990
miR-263a Regulates ENaC to Maintain Osmotic and Intestinal Stem Cell Homeostasis in Drosophila.
PMID:28017617
Modeling Monogenic Human Nephrotic Syndrome in the Drosophila Garland Cell Nephrocyte.
PMID:27932481
Exploring FlyBase Data Using QuickSearch.
PMID:27930807
FlyRNAi.org-the database of the Drosophila RNAi screening center and transgenic RNAi project: 2017 update.
PMID:27924039
WORMHOLE: Novel Least Diverged Ortholog Prediction through Machine Learning.
PMID:27812085
Cross-phenotype association tests uncover genes mediating nutrient response in Drosophila.
PMID:27809764
FlyBase at 25: looking to the future.
PMID:27799470
Using FlyBase, a Database of Drosophila Genes and Genomes.
PMID:27730573
RhoA GTPase inhibition organizes contraction during epithelial morphogenesis.
PMID:27551058
The translation factors of Drosophila melanogaster.
PMID:27494710
Comparative transcriptomic analysis of human and Drosophila extracellular vesicles.
PMID:27282340
Regulation of KAT6 Acetyltransferases and Their Roles in Cell Cycle Progression, Stem Cell Maintenance, and Human Disease.
PMID:27185879
Identification of Novel Regulators of the JAK/STAT Signaling Pathway that Control Border Cell Migration in the Drosophila Ovary.
PMID:27175018
A quantitative genome-wide RNAi screen in C. elegans for antifungal innate immunity genes.
PMID:27129311
Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology.
PMID:27113998
Controllability analysis of the directed human protein interaction network identifies disease genes and drug targets.
PMID:27091990
MECP2 impairs neuronal structure by regulating KIBRA.
PMID:27015692
Testing candidate genes for attention-deficit/hyperactivity disorder in fruit flies using a high throughput assay for complex behavior.
PMID:26954609
Modeling congenital disease and inborn errors of development in Drosophila melanogaster.
PMID:26935104
FlyBase portals to human disease research using Drosophila models.
PMID:26935103
The Genetic Basis for Variation in Sensitivity to Lead Toxicity in Drosophila melanogaster.
PMID:26859824
Zfrp8 forms a complex with fragile-X mental retardation protein and regulates its localization and function.
PMID:26772998
Genome-Wide Analysis Reveals Novel Regulators of Growth in Drosophila melanogaster.
PMID:26751788
Identification of Drosophila Zfh2 as a Mediator of Hypercapnic Immune Regulation by a Genome-Wide RNA Interference Screen.
PMID:26643480
Insights into ALS pathomechanisms: from flies to humans.
PMID:26594942
Conserved piRNA Expression from a Distinct Set of piRNA Cluster Loci in Eutherian Mammals.
PMID:26588211
Functional Conservation of the Glide/Gcm Regulatory Network Controlling Glia, Hemocyte, and Tendon Cell Differentiation in Drosophila.
PMID:26567182
An Orthologous Epigenetic Gene Expression Signature Derived from Differentiating Embryonic Stem Cells Identifies Regulators of Cardiogenesis.
PMID:26485529
Vilya, a component of the recombination nodule, is required for meiotic double-strand break formation in Drosophila.
PMID:26452093
Quantitative analysis of the murine lipid droplet-associated proteome during diet-induced hepatic steatosis.
PMID:26416795
Proteomic mapping in live Drosophila tissues using an engineered ascorbate peroxidase.
PMID:26362788
The Transgenic RNAi Project at Harvard Medical School: Resources and Validation.
PMID:26320097
PhosphOrtholog: a web-based tool for cross-species mapping of orthologous protein post-translational modifications.
PMID:26283093
Drosophila and Caenorhabditis elegans as Discovery Platforms for Genes Involved in Human Alcohol Use Disorder.
PMID:26173477
Beyond antioxidant genes in the ancient Nrf2 regulatory network.
PMID:26163000
GLAD: an Online Database of Gene List Annotation for Drosophila.
PMID:26157507
Network analyses reveal novel aspects of ALS pathogenesis.
PMID:25826266
Drosophila and experimental neurology in the post-genomic era.
PMID:25814441
Enhancer modeling uncovers transcriptional signatures of individual cardiac cell states in Drosophila.
PMID:25609699
EHFPI: a database and analysis resource of essential host factors for pathogenic infection.
PMID:25414353
Identification of genes associated with resilience/vulnerability to sleep deprivation and starvation in Drosophila.
PMID:25409104
A genetic screen identifies Tor as an interactor of VAPB in a Drosophila model of amyotrophic lateral sclerosis.
PMID:25361581
Combining genetic perturbations and proteomics to examine kinase-phosphatase networks in Drosophila embryos.
PMID:25284370
Genome-wide RNAi screen identifies the Parkinson disease GWAS risk locus SREBF1 as a regulator of mitophagy.
PMID:24912190
Resources for functional genomics studies in Drosophila melanogaster.
PMID:24653003
Functional screening in Drosophila identifies Alzheimer's disease susceptibility genes and implicates Tau-mediated mechanisms.
PMID:24067533
Conserved regulators of nucleolar size revealed by global phenotypic analyses.
PMID:23962978
Whole-genome sequencing uncovers the genetic basis of chronic mountain sickness in Andean highlanders.
PMID:23954164
FlyPrimerBank: an online database for Drosophila melanogaster gene expression analysis and knockdown evaluation of RNAi reagents.
PMID:23893746
UP-TORR: online tool for accurate and Up-to-Date annotation of RNAi Reagents.
PMID:23792952
Genetic determinants of phosphate response in Drosophila.
PMID:23520455
Protein complex-based analysis framework for high-throughput data sets.
PMID:23443684
A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease.
PMID:23032990
Neurological disorders: towards a mechanistic understanding of restless legs syndrome.
PMID:22720681
Mouse genetic and phenotypic resources for human genetics.
PMID:22422677
FlyRNAi.org--the database of the Drosophila RNAi screening center: 2012 update.
PMID:22067456
Proteomic and functional genomic landscape of receptor tyrosine kinase and ras to extracellular signal-regulated kinase signaling.
PMID:22028469